Chemical and charge characteristics of kaolinitic soils of south-east Queensland

Soil Research ◽  
1983 ◽  
Vol 21 (3) ◽  
pp. 271 ◽  
Author(s):  
JO Skjemstad ◽  
AJ Koppi
Keyword(s):  
Cation Exchange ◽  
Surface Area ◽  
Cation Exchange Capacity ◽  
Negative Charge ◽  
Ph Value ◽  
Divalent Cations ◽  
Active Surface ◽  
Exchange Capacity ◽  
Oxide Surface ◽  
Oxalate Extraction

Cation exchange capacity at field pH and net negative charge at pH 8.5 of 39 kaolinitic soils were studied in relation to surface area and other soil characteristics. All soils exhibited an anion exchange capacity at field pH, but this was very low compared with cation exchange capacity. Little evidence could be found for the presence of amorphous aluminium or silica, or short-range order alumino-silicates on the basis of acid oxalate-extraction, in contrast to Tiron extraction. All samples had significant permanent negative charge as deduced using the method of Gillman and Uehara, in addition to pHdependent charge. The former was strongly related to the exchangeable divalent cations, and this may explain the great variation in base saturation observed. Most of the charge in these soils is derived from the small poorly crystalline kaolins, although at high pH oxalate-extractable iron contributes significantly to the negative charge. Based on the results for those soils containing less than 5% iron oxide, surface area determined by ethylene glycol is linearly related to the net negative charge at pH 8.5. The average surface charge density on the soils containing <5% hematite and goethite measured at this pH value is 0.9 nm2/charge. Hematite and goethite show much lower negative charge densities and effectively dilute the active surface.

scholarly journals Effect of Low Zeolite Doses on Plants and Soil Physicochemical Properties

Materials ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2617
Author(s):  
Alicja Szatanik-Kloc ◽  
Justyna Szerement ◽  
Agnieszka Adamczuk ◽  
Grzegorz Józefaciuk
Keyword(s):  
Plant Growth ◽  
Physicochemical Properties ◽  
Cation Exchange ◽  
Surface Area ◽  
Cation Exchange Capacity ◽  
N Fertilization ◽  
Exchange Capacity ◽  
First Year ◽  
Soil Physicochemical Properties ◽  
Water Holding

Thousands of tons of zeolitic materials are used yearly as soil conditioners and components of slow-release fertilizers. A positive influence of application of zeolites on plant growth has been frequently observed. Because zeolites have extremely large cation exchange capacity, surface area, porosity and water holding capacity, a paradigm has aroused that increasing plant growth is caused by a long-lasting improvement of soil physicochemical properties by zeolites. In the first year of our field experiment performed on a poor soil with zeolite rates from 1 to 8 t/ha and N fertilization, an increase in spring wheat yield was observed. Any effect on soil cation exchange capacity (CEC), surface area (S), pH-dependent surface charge (Qv), mesoporosity, water holding capacity and plant available water (PAW) was noted. This positive effect of zeolite on plants could be due to extra nutrients supplied by the mineral (primarily potassium—1 ton of the studied zeolite contained around 15 kg of exchangeable potassium). In the second year of the experiment (NPK treatment on previously zeolitized soil), the zeolite presence did not impact plant yield. No long-term effect of the zeolite on plants was observed in the third year after soil zeolitization, when, as in the first year, only N fertilization was applied. That there were no significant changes in the above-mentioned physicochemical properties of the field soil after the addition of zeolite was most likely due to high dilution of the mineral in the soil (8 t/ha zeolite is only ~0.35% of the soil mass in the root zone). To determine how much zeolite is needed to improve soil physicochemical properties, much higher zeolite rates than those applied in the field were studied in the laboratory. The latter studies showed that CEC and S increased proportionally to the zeolite percentage in the soil. The Qv of the zeolite was lower than that of the soil, so a decrease in soil variable charge was observed due to zeolite addition. Surprisingly, a slight increase in PAW, even at the largest zeolite dose (from 9.5% for the control soil to 13% for a mixture of 40 g zeolite and 100 g soil), was observed. It resulted from small alterations of the soil macrostructure: although the input of small zeolite pores was seen in pore size distributions, the larger pores responsible for the storage of PAW were almost not affected by the zeolite addition.

Characteristics of variably saturated granular bentonite after long-term storage at near-field relevant temperatures

Clay Minerals ◽  
2013 ◽  
Vol 48 (2) ◽  
pp. 343-361 ◽  
Author(s):  
M. Valter ◽  
M. Plötze
Keyword(s):  
Physicochemical Properties ◽  
Cation Exchange ◽  
Surface Area ◽  
Cation Exchange Capacity ◽  
Elevated Temperatures ◽  
Near Field ◽  
Exchange Capacity ◽  
Hydraulic Permeability ◽  
Cation Composition ◽  
Retention Capacity

AbstractBentonite is a potential material for use in the engineered barrier of radioactive waste repositories because of its low hydraulic permeability, self-sealing capability and retention capacity. It is expected that bentonite would react at the elevated temperatures accompanying the radioactive decay in the nuclear waste. The presented study was started in order to improve understanding of the coupled influence of temperature and (pore) water on the physicochemical and mineralogical properties of bentonite during thermal treatment under near-field relevant conditions. Granular Na-bentonite MX-80 was differently saturated (Sr = 1–0.05) and stored at different temperatures (50–150°C) in a closed system. Upon dismantling after different periods of time (3 to 18 months), mineralogical characteristics, cation exchange capacity and content of leachable cations, as well as physicochemical properties such as surface area and water adsorption were investigated.The results showed a high mineralogical stability. A slight conversion from the sodium to an earth alkali form of the bentonite was observed. However, considerable changes in the physicochemical properties of the bentonite were observed, particularly by treatment above the critical temperature of 120°C. The cation exchange capacity decreased during heating at 150°C by approximately. 10%. The specific surface area dropped by more than 50%. The water uptake capacity under free swelling conditions showed a slight tendency to lower values especially for samples heated for more than 12 months. The water vapour adsorption ability in contrast drops by 25% already within three months at T = 120°C. These changes are mostly related to the variations in the interlayer cation composition and to smectite aggregation processes. The observed alterations are rather subtle. However, temperatures ⩾ 120°C had a remarkable negative influence on different properties of MX-80.

Cation exchange capacity of loess and overlying soil in the non-carbonate loess sections, North-Western Croatia

2013 ◽  
Vol 5 (4) ◽  
Author(s):  
Nenad Tomašić ◽  
Štefica Kampić ◽  
Iva Cindrić ◽  
Kristina Pikelj ◽  
Mavro Lučić ◽  
...  
Keyword(s):  
Organic Matter ◽  
Cation Exchange ◽  
Transition Zone ◽  
Cation Exchange Capacity ◽  
Clay Fraction ◽  
Sample Pretreatment ◽  
Loess Soil ◽  
Exchange Capacity ◽  
Oxalate Extraction ◽  
North Western

AbstractThe adsorption properties in terms of cation exchange capacity and their relation to the soil and sediment constituents (clay minerals, Fe-, Mn-, and Al-oxyhydroxides, organic matter) were investigated in loess, soil-loess transition zone, and soil at four loess-soil sections in North-Western Croatia. Cation exchange capacity of the bulk samples, the samples after oxalate extraction of Fe, Mn and Al, and after removal of organic matter, as well as of the separated clay fraction, was determined using copper ethylenediamine. Cation exchange capacity (pH∼7) of the bulk samples ranges from 5 to 12 cmolc/kg in soil, from 7 to 15 cmolc/kg in the soil-loess transition zone, and from 12 to 20 cmolc/kg in loess. Generally, CEC values increase with depth. Oxalate extraction of Fe, Mn, and Al, and removal of organic matter cause a CEC decrease of 3–38% and 8–55%, respectively, proving a considerable influence of these constituents to the bulk CEC values. In the separated clay fraction (<2 μm) CEC values are up to several times higher relative to those in the bulk samples. The measured CEC values of the bulk samples generally correspond to the clay mineral content identified. Also, a slight increase in muscovite/illite content with depth and the vermiculite occurrence in the loess horizon are concomitant with the CEC increase in deeper horizons, irrespective of the sample pretreatment.

Mineralogical study of clays from Dobrodo, Serbia, for use in ceramics

Clay Minerals ◽  
2019 ◽  
Vol 54 (4) ◽  
pp. 369-377 ◽  
Author(s):  
Maja Milošević ◽  
Predrag Dabić ◽  
Sabina Kovač ◽  
Lazar Kaluđerović ◽  
Mihovil Logar
Keyword(s):  
Specific Surface ◽  
Cation Exchange ◽  
Surface Area ◽  
Specific Surface Area ◽  
Cation Exchange Capacity ◽  
Mineralogical Composition ◽  
Exchange Capacity ◽  
Mineralogical Characterization ◽  
Mineralogical Study

AbstractThis study focuses on the mineralogical characterization of four raw clay samples from Dobrodo deposit, Serbia. Several analytical methods were applied to determine the chemical and mineralogical composition, morphology and physical properties (colour, plasticity, specific surface area, particle size and cation-exchange capacity) of the clay samples. Kaolinite, smectite and illite are the predominant phases in all of the samples studied that contain between 60.2 and 87.1 wt.% of clay. Quartz, feldspars, paragonite and Ti- and Fe-bearing phases were also identified. The relatively high SiO2/Al2O3 mass ratio indicates abundant quartz. The cation-exchange capacity of the samples varied between low and moderately charged clay minerals (12–52 mmol 100 g–1) with specific surface area values ranging from 94 to 410 m2 g–1. The plasticity index values (11–23%) suggest low to moderate plasticity. Preliminary results show that most of the raw clay from Dobrodo deposit might be suitable for use in ceramic applications.

scholarly journals Lab Study on the Effect of Cation Exchange Capacity on Slurry Performance in Slurry Shields

2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
By Pinghe Sun ◽  
Binkui Zhao ◽  
Han Cao ◽  
Jingyuan Wang ◽  
Dingqiang Mo ◽  
...  
Keyword(s):  
Cation Exchange ◽  
Rheological Properties ◽  
Cation Exchange Capacity ◽  
Ph Value ◽  
Field Work ◽  
Exchange Capacity ◽  
Rheological Parameters ◽  
Flow Index ◽  
Linear Change ◽  
Design Requirements

Ion stabilizers can enhance the reinforcement slurry effect on the wall and stabilize the wall actively in slurry shields. This paper presents different cation exchange capacities obtained by changing the content of the ion stabilizer (1.5%, 2.0%, 2.5%, 3.0%, 3.5%, 4.0%, 4.5%, 5.0%, 5.5%, and 6.0%) in slurry associated with the basis of the existing slurry formula through the laboratory tests. In order to study the effect of the cation exchange capacity on the performance of slurry properties, the rheological properties of the slurry are analyzed and evaluated by the power law model. Results indicate that the cation exchange capacity of the slurry decreases first and then increases with the increase of the ion stabilizer content. When the content of the ion stabilizer is maintained at 3.50%, the cation exchange capacity reaches the minimum value of 2.92. The filtration volumes, pH values, and rheological parameters of the slurry also indicate an obvious linear change with the change of the cation exchange capacity. The minimum filtration volume is 9.70 mL/30 min when the ion stabilizer content reaches 3.50%. However, the pH value reaches the maximum, that is, 11.34 which is changed from 10, and the change could be considered as a constant value in the field work. When the cation exchange capacity increases, the continuity of polymer structure in the slurry decreases first and then increases, the flow index and consistency coefficient are located within a reasonable range, and the rheological properties of the slurry meet the design requirements of the standards.

scholarly journals Analysis of the sorption properties of different soils using water vapour adsorption and potentiometric titration methods

2016 ◽  
Vol 30 (3) ◽  
pp. 369-374 ◽  
Author(s):  
Kamil Skic ◽  
Patrycja Boguta ◽  
Zofia Sokołowska
Keyword(s):  
Specific Surface ◽  
Cation Exchange ◽  
Surface Charge ◽  
Surface Area ◽  
Water Vapour ◽  
Potentiometric Titration ◽  
Specific Surface Area ◽  
Cation Exchange Capacity ◽  
Exchange Capacity ◽  
Sorption Properties

Abstract Parameters of specific surface area as well as surface charge were used to determine and compare sorption properties of soils with different physicochemical characteristics. The gravimetric method was used to obtain water vapour isotherms and then specific surface areas, whereas surface charge was estimated from potentiometric titration curves. The specific surface area varied from 12.55 to 132.69 m2 g−1 for Haplic Cambisol and Mollic Gleysol soil, respectively, and generally decreased with pH (R=0.835; α = 0.05) and when bulk density (R=−0.736; α = 0.05) as well as ash content (R=−0.751; α = 0.05) increased. In the case of surface charge, the values ranged from 63.00 to 844.67 μmol g−1 Haplic Fluvisol and Mollic Gleysol, respecively. Organic matter gave significant contributions to the specific surface area and cation exchange capacity due to the large surface area and numerous surface functional groups, containing adsorption sites for water vapour molecules and for ions. The values of cation exchange capacity and specific surface area correlated linearly at the level of R=0.985; α = 0.05.

INFLUENCE OF CLAY MINERALS ON MICROORGANISMS: III. EFFECT OF PARTICLE SIZE, CATION EXCHANGE CAPACITY, AND SURFACE AREA ON BACTERIA

1966 ◽  
Vol 12 (6) ◽  
pp. 1235-1246 ◽  
Author(s):  
G. Stotzky
Keyword(s):  
Particle Size ◽  
Cation Exchange ◽  
Surface Area ◽  
Clay Minerals ◽  
Cation Exchange Capacity ◽  
Physicochemical Characteristics ◽  
Exchange Capacity ◽  
Bacterial Respiration ◽  
Effect Of Particle Size ◽  
Stimulation Of

The stimulation of bacterial respiration by clay minerals was related to certain physicochemical characteristics of clays. Respiration increased with an increase in the cation exchange capacity and surface area of the particles. The importance of surface area, however, could not be unequivocally established, as some of the methods used to determine this characteristic on certain clay species were questionable. Particle size did not appear to be a critical characteristic. The implications of the cation exchange capacity of clay minerals in the activity, ecology, and population dynamics of microorganisms in nature are discussed.

Sign in / Sign up

Export Citation Format

Share Document